Results 11 to 20 of about 133,122 (299)

Induced terpene accumulation in Norway spruce inhibits bark beetle colonization in a dose-dependent manner. [PDF]

open access: yesPLoS ONE, 2011
Tree-killing bark beetles (Coleoptera, Scolytinae) are among the most economically and ecologically important forest pests in the northern hemisphere. Induction of terpenoid-based oleoresin has long been considered important in conifer defense against ...
Tao Zhao   +7 more
doaj   +3 more sources

Phylogenomic analyses and distribution of terpene synthases among Streptomyces [PDF]

open access: yesBeilstein Journal of Organic Chemistry, 2019
Terpene synthases are widely distributed among microorganisms and have been mainly studied in members of the genus Streptomyces. However, little is known about the distribution and evolution of the genes for terpene synthases.
Lara Martín-Sánchez   +5 more
doaj   +3 more sources

Tuberculosis Terpene Targets

open access: yesChemistry & Biology, 2015
In this issue, Young, Moody, and colleagues report the discovery of an isomer of the Mycobacterium tuberculosis (Mtb) virulence factor 1-tuberculosinyl adenosine, N(6)-tuberculosinyl adenosine, in mice infected with tuberculosis. These Mtb-derived terpene compounds may serve as sensitive and specific biomarkers of infection.
Oldfield, Eric
openaire   +3 more sources

The Cannabis Terpenes [PDF]

open access: yesMolecules, 2020
Terpenes are the primary constituents of essential oils and are responsible for the aroma characteristics of cannabis. Together with the cannabinoids, terpenes illustrate synergic and/or entourage effect and their interactions have only been speculated in for the last few decades.
Sarana Rose Sommano   +3 more
openaire   +3 more sources

First trans-eunicellane terpene synthase in bacteria

open access: yes, 2022
Terpenoids are the largest family of natural products, but prokaryotes are vastly underrepresented in this chemical space. However, genomics supports vast untapped biosynthetic potential for terpenoids in bacteria.
Donovon, Adpressa   +10 more
core   +1 more source

Terpene Cyclase Mimicking Chlorine-Induced Polyene Cyclizations

open access: yes, 2022
Nature forges a plethora of structurally divers polyenes with high efficiency and selectivity in a single cyclization step from achiral precursor. Imitating this powerful strategy has been the subject of numerous synthetic efforts.
Julia, Binder, Tanja, Gulder
core   +1 more source

Terpenoids From Cannabis Do Not Mediate an Entourage Effect by Acting at Cannabinoid Receptors

open access: yesFrontiers in Pharmacology, 2020
The entourage effect was a proposed explanation for biological observations that endocannabinoid ligand activities can be modified by other lipids released from cells at the same time.
David B. Finlay   +4 more
doaj   +1 more source

Unraveling the role of prenyl side-chain interactions in stabilizing the secondary carbocation in the biosynthesis of variexenol B

open access: yesBeilstein Journal of Organic Chemistry, 2023
Terpene cyclization reactions involve a number of carbocation intermediates. In some cases, these carbocations are stabilized by through-space interactions with π orbitals.
Moe Nakano, Rintaro Gemma, Hajime Sato
doaj   +1 more source

Genomic Insights of Halophilic Planococcus maritimus SAMP MCC 3013 and Detail Investigation of Its Biosurfactant Production

open access: yesFrontiers in Microbiology, 2019
Moderate halophilic bacteria thrive in saline conditions and produce biosurfactant (BS) which facilitates the oil scavenging activity in the oil polluted surroundings.
Samadhan Waghmode   +7 more
doaj   +1 more source

Discovery and Characterization of a Terpene Biosynthetic Pathway featuring a Norbornene-forming Diels-Alderase

open access: yes, 2022
Pericyclases, enzymes that catalyze pericyclic reactions, form an expanding family of enzymes that have biocatalytic utility. Despite the increasing number of pericyclases discovered, the Diels-Alder (DA) cyclization between a cyclopentadiene and an ...
Kendall, Houk   +4 more
core   +1 more source

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